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  • How to Reduce Internal Stress of Nylon Injection Molded Parts Through Modification
    How to Reduce Internal Stress of Nylon Injection Molded Parts Through Modification
    Sep 11, 2025
    Nylon materials are highly susceptible to internal stress during injection molding, primarily due to molecular orientation, uneven cooling shrinkage, and poor additive dispersion. Excessive internal stress can lead to deformation, cracking, and deterioration of performance. To address this issue, modification technologies play a critical role. On the molecular level, incorporating flexible segments or impact modifiers helps reduce brittleness and mitigate stress concentration. Commonly used toughening agents include elastomers, thermoplastic elastomers, or graft-modified materials, which form phase-separated structures within the nylon matrix, effectively absorbing and redistributing stress. Glass fiber reinforcement significantly improves the strength and rigidity of nylon, yet it can also introduce internal stress. Controlling fiber length, content, and distribution is essential. While long fibers provide higher strength, they also induce greater shrinkage differences during cooling. Short fibers can improve dimensional stability, and surface treatments with coupling agents can enhance interfacial compatibility, thus minimizing stress concentration. From a processing perspective, mold design and molding parameters are equally important. Gate position, cooling system design, and molding temperature and pressure curves determine stress distribution within the part. Proper gate design ensures uniform melt flow and reduces molecular orientation. Higher mold temperatures extend relaxation time for molecular chains, lowering residual stress. Post-molding annealing is another effective approach, allowing molecular chains to rearrange under conditions near nylon’s glass transition temperature, thereby relieving residual stress from rapid cooling. In terms of additive systems, lubricants and nucleating agents can also be applied. Lubricants improve melt flowability and reduce friction-induced defects, while nucleating agents regulate crystallization rate and grain size, ensuring uniform shrinkage during cooling and minimizing stress concentration. All in all, reducing internal stress in nylon injection molded parts requires a combination of material modification and process optimization. Toughening, reinforcement, lubrication, and crystallization control can enhance stress distribution on a molecular level, while appropriate molding parameters and post-processing further stabilize performance. This integrated approach not only enhances the application value of nylon but also lays the foundation for its adoption in high-performance engineering applications.
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  • What is Modified Nylon? The Evolution Path of Materials Starting from PA6/PA66
    What is Modified Nylon? The Evolution Path of Materials Starting from PA6/PA66
    Aug 15, 2025
    Nylon, as a key engineering plastic, has evolved from a general-purpose material to a variety of performance-adjustable modified products since its invention in the last century. Among them, PA6 and PA66 are the most common base types. Although their molecular structures are similar, their performance differs slightly. PA66 has advantages in crystallinity, heat resistance, and rigidity, while PA6 offers better toughness and different moisture absorption characteristics. In the early stage of industrialization, these materials were mainly used in their virgin form for fibers, gears, and bearings. However, as industrial demands increased, single-property nylon materials could no longer meet complex application requirements, leading to the emergence of modified nylon. Modified nylon is produced by physically or chemically adjusting the performance of base PA6 or PA66. Common modification methods include reinforcement, toughening, flame retardancy, wear resistance, and weather resistance. Reinforcement often involves adding glass fibers, carbon fibers, or mineral fillers to improve mechanical strength and dimensional stability. Toughening typically uses elastomeric rubbers to enhance low-temperature impact resistance. Flame retardant modification introduces phosphorus- or nitrogen-based systems into the polymer structure to meet safety standards in the electrical and electronics industries. These modifications not only alter physical properties but also expand nylon’s application boundaries in automotive, home appliances, electronics, and industrial machinery. The evolution of these materials is driven by application requirements. For example, components in automotive engine compartments must operate for long periods under high temperatures and exposure to oil, demanding excellent heat stability, chemical resistance, and mechanical strength. Traditional PA6 or PA66 would degrade under such conditions, while glass fiber-reinforced and heat-stabilized nylon maintains its performance. In the electronics sector, components such as sockets and switches require flame retardancy while maintaining electrical insulation and dimensional accuracy, which has driven the widespread adoption of flame-retardant reinforced nylon. The development of modified nylon is also closely tied to advances in processing technology. Modern modification processes go beyond traditional twin-screw compounding to include nano-filler dispersion technology, reactive extrusion, and intelligent formulation design, enabling balanced performance while maintaining uniformity and processability. This synergy between materials and processing allows modified nylon to be tailored precisely for specific applications rather than serving as a simple universal replacement. From the virgin forms of PA6 and PA66 to the wide variety of modification options available today, the evolution of these materials reflects the broader trend in the engineering plastics industry toward diversified performance and specialized applications. In the future, with the deepening focus on sustainability and the circular economy, modification technologies based on recycled nylon will become a research hotspot, achieving a balance between material performance and environmental requirements. This represents not only scientific progress in materials but also a shift of the entire value chain toward higher added value.
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